A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3226358



Internal ID22369191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:57403194..57403257hg38UCSC Ensembl
chr14:57869912..57869975hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14369505, nssv14369504
SamplesHG00731, HG00732
Known GenesNAA30
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3226358
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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